10 research outputs found

    Pilot Beam Sequence Design for Channel Estimation in Millimeter-Wave MIMO Systems: A POMDP Framework

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    In this paper, adaptive pilot beam sequence design for channel estimation in large millimeter-wave (mmWave) MIMO systems is considered. By exploiting the sparsity of mmWave MIMO channels with the virtual channel representation and imposing a Markovian random walk assumption on the physical movement of the line-of-sight (LOS) and reflection clusters, it is shown that the sparse channel estimation problem in large mmWave MIMO systems reduces to a sequential detection problem that finds the locations and values of the non-zero-valued bins in a two-dimensional rectangular grid, and the optimal adaptive pilot design problem can be cast into the framework of a partially observable Markov decision process (POMDP). Under the POMDP framework, an optimal adaptive pilot beam sequence design method is obtained to maximize the accumulated transmission data rate for a given period of time. Numerical results are provided to validate our pilot signal design method and they show that the proposed method yields good performance.Comment: 6 pages, 6 figures, submitted to IEEE ICC 201

    Reverse Signaling of Tumor Necrosis Factor Superfamily Proteins in Macrophages and Microglia: Superfamily Portrait in the Neuroimmune Interface

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    The tumor necrosis factor (TNF) superfamily (TNFSF) is a protein superfamily of type II transmembrane proteins commonly containing the TNF homology domain. The superfamily contains more than 20 protein members, which can be released from the cell membrane by proteolytic cleavage. Members of the TNFSF function as cytokines and regulate diverse biological processes, including immune responses, proliferation, differentiation, apoptosis, and embryogenesis, by binding to TNFSF receptors. Many TNFSF proteins are also known to be responsible for the regulation of innate immunity and inflammation. Both receptor-mediated forward signaling and ligand-mediated reverse signaling play important roles in these processes. In this review, we discuss the functional expression and roles of various reverse signaling molecules and pathways of TNFSF members in macrophages and microglia in the central nervous system (CNS). A thorough understanding of the roles of TNFSF ligands and receptors in the activation of macrophages and microglia may improve the treatment of inflammatory diseases in the brain and periphery. In particular, TNFSF reverse signaling in microglia can be exploited to gain further insights into the functions of the neuroimmune interface in physiological and pathological processes in the CNS

    Filter-and-Forward Transparent Relay Design for OFDM Systems

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    Cathelicidin-Related Antimicrobial Peptide Negatively Regulates Bacterial Endotoxin-Induced Glial Activation

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    Recent studies have suggested that mouse cathelicidin-related antimicrobial peptide (CRAMP) and its human homologue leucine leucine-37 (LL-37) play critical roles in innate immune responses. Here, we studied the role of mouse CRAMP in bacterial endotoxin lipopolysaccharide (LPS)-induced neuroinflammation. CRAMP peptide treatment significantly inhibited LPS-mediated inflammatory activation of glial cells in culture. In the animal model of LPS-induced neuroinflammation, CRAMP expression was highly induced in multiple cell types, such as astrocytes, microglia, and neurons. Injection of exogenous CRAMP peptide significantly inhibited inflammatory cytokine expression and the reactivity of glial cells in the mouse brain following intraperitoneal or intracerebroventricular LPS administration. Altogether, results of the study suggest that CRAMP plays an important part in containment of LPS-induced neuroinflammatory responses, and that CRAMP can be exploited for the development of targeted therapies for neuroinflammatory conditions associated with bacterial infection

    Robust Trajectory Planning for a Multirotor against Disturbance based on Hamilton-Jacobi Reachability Analysis

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    Ensuring safety in trajectory planning of multirotor systems is an essential element for risk-free operation. Even if the generated trajectory is known to be safe in the planning phase, unknown disturbance during an actual operation can lead to a dangerous situation. This paper proposes safety-guaranteed receding horizon planning against unknown, but bounded, disturbances. We first characterize forward reachable set (FRS) of the system, the set of states after a certain duration considering all possible disturbances, using Hamilton-Jacobi (HJ) reachability analysis. To compute the FRSs in real-time, we conservatively approximate the true FRS and perform ellipsoidal parameterization on the FRSs. Using the FRSs, we can plan a robust trajectory that avoids risky regions and rapidly re-plan the trajectory when the system encounters sudden disturbance. The proposed method is validated through an experiment of avoiding obstacles in a wind.N

    Characterization of Mesenchymal Stem Cells Derived from Patients with Cerebellar Ataxia: Downregulation of the Anti-Inflammatory Secretome Profile

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    Mesenchymal stem cell (MSC) therapy is a promising alternative approach for the treatment of neurodegenerative diseases, according to its neuroprotective and immunomodulatory potential. Despite numerous clinical trials involving autologous MSCs, their outcomes have often been unsuccessful. Several reports have indicated that MSCs from patients have low capacities in terms of the secretion of neurotrophic or anti-inflammatory factors, which might be associated with cell senescence or disease severity. Therefore, a new strategy to improve their capacities is required for optimal efficacy of autologous MSC therapy. In this study, we compared the secretory potential of MSCs among cerebellar ataxia patients (CA-MSCs) and healthy individuals (H-MSCs). Our results, including secretome analysis findings, revealed that CA-MSCs have lower capacities in terms of proliferation, oxidative stress response, motility, and immunomodulatory functions when compared with H-MSCs. The functional differences were validated in a scratch wound healing assay and neuron-glia co-cultures. In addition, the neuroprotective and immunoregulatory protein follistatin-like 1 (FSTL1) was identified as one of the downregulated proteins in the CA-MSC secretome, with suppressive effects on proinflammatory microglial activation. Our study findings suggest that targeting aspects of the downregulated anti-inflammatory secretome, such as FSTL1, might improve the efficacy of autologous MSC therapy for CA

    A Kinetic Indicator of Ultrafast Nickel-Rich Layered Oxide Cathodes

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    Elucidating high-rate cycling-induced nonequilibriumelectrodereactions is crucial for developing extreme fast charging (XFC) batteries.Herein, we unveiled the distinct rate capabilities of a series ofNi-rich layered oxide (NRLO) cathodes by quantitatively establishingtheir dynamic structure-kinetics relationships. Contrary toconventional views, we discovered electrode kinetic properties obtained ex-situ near equilibrium states failed to assess the effectiverate capability of NRLOs at ultrafast C rates. Further, the kineticphase heterogeneity, characterized by the dynamic separations in in-situ X-ray diffraction patterns and deviations in NRLO c-axis lattice parameters, exclusively correlated with thecapacity reduction under XFC and became an effective indicator ofthe NRLO rate capability. Enhancing the cycling temperature boostedthe rate capability of studied NRLOs by similar to 10%, which was furtherverified to mitigate the kinetic phase heterogeneity during XFC. Overall,this study lays the groundwork for tuning the kinetic phase heterogeneityof electrodes to develop ultrafast batteries.N

    A Kinetic Indicator of Ultrafast Nickel-Rich Layered Oxide Cathodes

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    Elucidating high-rate cycling-induced nonequilibrium electrode reactions is crucial for developing extreme fast charging (XFC) batteries. Herein, we unveiled the distinct rate capabilities of a series of Ni-rich layered oxide (NRLO) cathodes by quantitatively establishing their dynamic structure–kinetics relationships. Contrary to conventional views, we discovered electrode kinetic properties obtained ex-situ near equilibrium states failed to assess the effective rate capability of NRLOs at ultrafast C rates. Further, the kinetic phase heterogeneity, characterized by the dynamic separations in in-situ X-ray diffraction patterns and deviations in NRLO c-axis lattice parameters, exclusively correlated with the capacity reduction under XFC and became an effective indicator of the NRLO rate capability. Enhancing the cycling temperature boosted the rate capability of studied NRLOs by ∼10%, which was further verified to mitigate the kinetic phase heterogeneity during XFC. Overall, this study lays the groundwork for tuning the kinetic phase heterogeneity of electrodes to develop ultrafast batteries
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